Scientific & QA Jobs

Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead

IQVIA • Reading, Berkshire

Salary

£57k – £57k

Posted

22 July 2026

Work mode

Full-time

Sponsor match

high

Global Business Mobility: Senior or Specialist WorkerWorker (A rating)

Role overview

IQVIA is hiring a Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead in Reading, a full-time scientific & qa role. The advertised salary is £57k – £57k. IQVIA holds an active licence on the UK Home Office register of sponsors for the Global Business Mobility: Senior or Specialist Worker route, which means it can sponsor a visa for this hire if it chooses to.

Job Overview The Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effective inspection readiness programs, and successful management of inspections and audits. Key responsibilities includ…

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Visa sponsorship snapshot

Employer: IQVIA — confirmed licensed sponsor
Visa route: Global Business Mobility: Senior or Specialist Worker
Advertised salary: £57k – £57k
How this salary compares: about 40% above the £40,494 median across 994 scientific & qa roles with published salaries on FindSponsorJobs
Location: Reading, Berkshire · Full-time
Similar roles nearby: 30 other live scientific & qa roles in Reading — browse them
Posted: 22 July 2026
How we verify sponsors: employers are matched against the UK Home Office register of licensed sponsors — read our methodology.

About this sector

Scientific and quality assurance roles span pharmaceutical, biotech, clinical research, and laboratory sectors. The UK life sciences industry actively recruits internationally for research scientists, QA managers, regulatory affairs specialists, and clinical trial coordinators, with many employers maintaining well-established sponsor licence operations.